FDA Adverse Event Malfunction Summary report: N

OT PING METER

MDR report key: 1871740 · Received October 15, 2010

Report

Report Number
2939301-2010-09121
Event Type
Malfunction
Date Received
October 15, 2010
Report Date
October 10, 2010
Manufacturer
LIFESCAN, INC.
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

THE 510 (K) # IS K082590.

Description of Event or Problem · 1

THE LAY USER/PATIENT CONTACTED LIFESCAN ALLEGING THE METER DOES NOT POWER ON WITH STRIP INSERTION OR BY PRESSING BUTTONS. THE ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WERE NO ALLEGATIONS OF HARM OR INJURY. REPLACEMENT PRODUCTS WERE SENT TO THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OT PING METER GLUCOSE MONITORING SYS/KIT NBW LIFESCAN, INC. 3028092

Patients

Seq Age Sex Outcome Treatment
1 14 YR